Update on the clinical management of Wilson's disease

Update on the clinical management of Wilson's disease

Peter Hedera Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA Abstract: Wilson’s disease (WD), albeit relatively rare, is an important genetic metabolic disease because of highly effective therapies that can be lifesaving. It is a great imitator and require...

Full description

Bibliographic Details
Main Author:	Hedera P
Format:	Article
Language:	English
Published:	Dove Medical Press 2017-01-01
Series:	The Application of Clinical Genetics
Subjects:	Wilson’s disease copper ATP7B chelation gene therapy
Online Access:	https://www.dovepress.com/update-on-the-clinical-management-of-wilson39s-disease-peer-reviewed-article-TACG

Similar Items

Wilson’s Disease: An Update on the Diagnostic Workup and Management
by: Beata Kasztelan-Szczerbinska, et al.
Published: (2021-10-01)

Biochemical diagnosis of Wilson’s disease: an update
by: Martínez-Morillo Eduardo, et al.
Published: (2022-04-01)

Wilson Disease: Update on Pathophysiology and Treatment
by: Som Dev, et al.
Published: (2022-05-01)

Clinical and Genetic Analysis in Neurological Wilson’s Disease Patients With Neurological Worsening Following Chelator Therapy
by: Haiman Hou, et al.
Published: (2022-04-01)

Clinical and genetic heterogeneity in Wilson disease - A review
by: Advithi Rangaraju, et al.
Published: (2015-09-01)

Research progress in stem cell therapy for Wilson disease
by: Xianlang Xiong, et al.
Published: (2024-12-01)

Exploring the potential of trientine tetrahydrochloride in the treatment of Wilson disease
by: Nikita Sharma, et al.
Published: (2023-03-01)

Wilson disease – a case report
by: Simina Cozma, et al.
Published: (2018-06-01)

New ATP7B Gene Mutation in a Brazilian Patient with Wilson Disease
by: Marcus Villander Barros de Oliveira Sá, et al.
Published: (2022-12-01)

High value of 64Cu as a tool to evaluate the restoration of physiological copper excretion after gene therapy in Wilson’s disease
by: Oihana Murillo, et al.
Published: (2022-09-01)

Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified
by: Zhongyan Xiao, et al.
Published: (2021-09-01)

Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients
by: Karima Lafhal, et al.
Published: (2023-09-01)

The Role of Zinc in the Treatment of Wilson’s Disease
by: Abolfazl Avan, et al.
Published: (2022-08-01)

Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype
by: Annamaria Sapuppo, et al.
Published: (2020-06-01)

Acute-Onset Visual Impairment in Wilson's Disease: A Case Report and Literature Review
by: Zi-Wei Zheng, et al.
Published: (2022-06-01)

Study of T991T polymorphism in Cuban patients with clinical diagnosis of Wilson’s disease
by: Yulia Clark, et al.
Published: (2016-09-01)

Neurological Wilson’s Disease Signs—Hepatic Encephalopathy or Copper Toxicosis?
by: Anna Jopowicz, et al.
Published: (2023-02-01)

High genetic carrier frequency of Wilson’s disease in France: discrepancies with clinical prevalence
by: Corinne Collet, et al.
Published: (2018-08-01)

Currently Clinical Views on Genetics of Wilson′s Disease
by: Chen Chen, et al.
Published: (2015-01-01)

Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease
by: Nguyen Thi Mai Huong, et al.
Published: (2018-06-01)

Mutation analysis of the ATP7B gene and genotype–phenotype correlation in Chinese patients with Wilson disease
by: Mingming Li, et al.
Published: (2021-09-01)

Benefits and drawbacks of current copper chelators in Wilson disease
by: Ioan-Cristian Lupescu, et al.
Published: (2023-03-01)

Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report
by: Omid Daneshjoo, et al.
Published: (2018-03-01)

Liver Failure of Wilson's Disease With Manifestations Similar to Porphyria and Uncommon ATP7B Gene Mutation: A Case Report and Literature Review
by: Ju Zou, et al.
Published: (2021-07-01)

Screening of Wilson’s disease in a psychiatric population: difficulties and pitfalls. A preliminary study
by: Caroline Demily, et al.
Published: (2017-04-01)

Mutation spectrum of ATP7B gene in pediatric patients with Wilson disease in Vietnam
by: Nguyen Thi Mai Huong, et al.
Published: (2022-06-01)

Phenotypic polymorphism in Wilson’s disease – between genetics and epigenetics
by: Veronica Cumpata
Published: (2022-09-01)

Novel mutations in ATP7B gene of Wilson\'s disease in Iranian patients
by: Iradj Maleki, et al.
Published: (2013-02-01)

A Novel Splice-site Allelic Variant is Responsible for Wilson Disease in an Omani Family
by: Mohammed Al-Tobi, et al.
Published: (2011-12-01)

Wilson’s Disease: Facing the Challenge of Diagnosing a Rare Disease
by: Ana Sánchez-Monteagudo, et al.
Published: (2021-08-01)

FOUR DIFFERENT PRESENTATIONS OF WILSON’S DISEASE IN ONE FAMILY
by: Asbah Rahman, et al.
Published: (2021-08-01)

Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis
by: Jonathon eTelianidis, et al.
Published: (2013-08-01)

Enfermedad de Wilson. Actualidad del tema
by: Yulia Clark Feoktistova

First application of next-generation sequencing in four families with Wilson disease in Morocco
by: Maryem Sahli, et al.
Published: (2023-09-01)

Investigation of Genetic Modifiers of Copper Toxicosis in Labrador Retrievers
by: Xiaoyan Wu, et al.
Published: (2020-10-01)

Wilson’s disease
by: Hursitoglu Mehmet, et al.
Published: (2010-04-01)

The Specific Copper(II) Chelator TDMQ20 Is Efficient for the Treatment of Wilson’s Disease in Mice
by: Yingshan Zhu, et al.
Published: (2023-12-01)

Advance in the pathogenesis and treatment of Wilson disease
by: Dong Qin-Yun, et al.
Published: (2012-11-01)

A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease
by: France Woimant, et al.
Published: (2020-10-01)

The mutation spectrum and ethnic distribution of Wilson disease, a review
by: Zahra Beyzaei, et al.
Published: (2024-03-01)